Primary Site >> Esophagus Cancer

Gene >> C2orf40

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000238044
Start 106073939:106073939(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.181T>G
AA Mutation p.Phe61Val(p.F61V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000238044
Start 106073914:106073914(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.156C>T
Mutation Classification Silent
Feature Type Transcript